Aripiprazole for drug-induced psychosis in Parkinson disease: Preliminary experience

被引:87
作者
Fernandez, HH
Trieschmann, ME
Friedman, JH
机构
[1] Univ Florida, McKnight Brain Inst, Coll Med, Dept Neurol, Gainesville, FL 32610 USA
[2] Brown Univ, Sch Med, Dept Clin Neurosci, Providence, RI 02912 USA
关键词
D O I
10.1097/00002826-200401000-00003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Aripiprazole is the newest atypical antipsychotic (AA) drug to be released in the US. It is the only AA that is a partial agonist at the D2 and 5HT1a receptors and an antagonist at 5HT2a receptors. It also has a high 5HT2/D2 ratio and may therefore carry a low risk of extrapyramidal side effects and alleviate psychosis in Parkinson-vulnerable populations. We report our preliminary experience in 8 patients with probable Parkinson disease (PD) treated with aripiprazole for drug-induced psychosis. Two patients were neuroleptic-naive, 5 patients were "quetiapine failures", and 1 patient was switched from olanzapine to aripiprazole. Aripiprazole was started at 5 mg to 10 mg a day and slowly increased over 3 to 7 days until side effects or improvement of psychosis occurred. Only 2 out of 8 patients experienced near complete resolution of their psychosis using aripiprazole. The other six patients discontinued aripiprazole within 40 days, 2 of whom discontinued due to motor worsening. Our preliminary experience with aripiprazole is mixed but not very encouraging. Controlled studies are needed to evaluate aripiprazole in parkinsonian patients.
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页码:4 / 5
页数:2
相关论文
共 9 条
[1]  
*COMP BMS, 2002, OTS AM PHARM
[2]   The role of atypical antipsychotics in the treatment of movement disorders [J].
Fernandez, HH ;
Friedman, JH .
CNS DRUGS, 1999, 11 (06) :467-483
[3]   Treatment of psychosis in Parkinson's disease - Safety considerations [J].
Fernandez, HH ;
Trieschmann, ME ;
Friedman, JH .
DRUG SAFETY, 2003, 26 (09) :643-659
[4]   Long-term outcome of quetiapine use fox psychosis among Parkinsonian patients [J].
Fernandez, HH ;
Trieschmann, ME ;
Burke, MA ;
Jacques, C ;
Friedman, JH .
MOVEMENT DISORDERS, 2003, 18 (05) :510-514
[5]   5-HT2A and D2 receptor blockade increases cortical DA release via 5-HT1A receptor activation:: a possible mechanism of atypical antipsychotic-induced cortical dopamine release [J].
Ichikawa, J ;
Ishii, H ;
Bonaccorso, S ;
Fowler, WL ;
O'Laughlin, IA ;
Meltzer, HY .
JOURNAL OF NEUROCHEMISTRY, 2001, 76 (05) :1521-1531
[6]   Does fast dissociation from the dopamine D2 receptor explain the action of atypical antipsychotics?:: A new hypothesis [J].
Kapur, S ;
Seeman, P .
AMERICAN JOURNAL OF PSYCHIATRY, 2001, 158 (03) :360-369
[7]  
MELTZER H, 1989, PSYCHOPHARMACOLOGY B, P25
[8]   Action of atypical antipsychotics [J].
Meltzer, HY .
AMERICAN JOURNAL OF PSYCHIATRY, 2002, 159 (01) :153-154
[9]   Diagnostic and Statistical Manual of Mental Disorders [J].
Mittal, Vijay A. ;
Walker, Elaine F. .
PSYCHIATRY RESEARCH, 2011, 189 (01) :158-159